Simultaneous determination of one- and two-bond scalar and residual dipolar couplings between 13C′, 13Cα, and 15N spins in proteins

被引:3
|
作者
Puttonen, Eetu [1 ]
Tossavainen, Helena [1 ]
Permi, Perttu [1 ]
机构
[1] Univ Helsinki, NMR Lab, Inst Biotechnol, Program Struct Biol & Biophys, FI-00014 Helsinki, Finland
关键词
coactosin; J couplings; Karplus parameterization; NMR spectroscopy; proteins; residual dipolar couplings; TSR-1 domain of F-spondin; ubiquitin;
D O I
10.1002/mrc.1836
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Four simple and sensitive HNCO-based methods for measurement of (1)J(C)'(alpha)(C), (1)J(NC)(alpha) and (2)J(NC)(alpha) coupling constants in protein main chains are presented. Three of these experiments enable the simultaneous measurement of (1)J(C'C)(alpha), (1)J(NC)(alpha) and (2)J(NC)(alpha) couplings. Exploitation of the E.COSY principle provides excellent dispersion of cross peaks in, the resulting 3D spectra. The couplings can be retrieved with good accuracy from peak-to-peak separations. Karplus parameterizations are provided for (1)J(NC)(alpha) and (2)J(NC)(alpha) obtained from a nearly complete set of couplings of human ubiquitin. In addition, feasibility of the proposed methodology for measuring several residual dipolar couplings (RDCs) simultaneously is assessed. Copyright (C) 2006 John Wiley & Sons, Ltd.
引用
收藏
页码:S168 / S176
页数:9
相关论文
共 50 条